bibliographic entry 1067548 [be/1067548]
https://w3id.org/oc/corpus/be/1067548

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  • Lupoglazoff JM, Cheav T, Baroudi G, Berthet M, Denjoy I, Cauchemez B, Extramiana F, Chahine M, Guicheney P. Homozygous SCN5A mutation in long‐QT syndrome with functional two‐to‐ one atrioventricular block. Circ Res. 2001; 89: E16–E21. PMID: 11463728
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